Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.
- NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_assertion description "[these findings identify RNF11 as a strong candidate gene at the PARK10 locus and highlight its potential significance in the development of the common form of Parkinson disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.
- NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_assertion evidence source_evidence_literature NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.
- NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_assertion SIO_000772 17917589 NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.
- NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_assertion wasDerivedFrom lhgdn-20090331 NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.
- NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_assertion wasGeneratedBy ECO_0000203 NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP130693.RAk0VqG0usdoFbmy6PPD1_53V6_o-8rVfYPH8bhSuleeE130_provenance.